Literature DB >> 8568717

9p-Syndrome.

J Boby1, S C Karande, K R Lahiri, M K Jain, S Kanade.   

Abstract

A 2 1/2 month old male child was admitted with loose motions and mild dehydration. He was full term normal delivery, born of a non-consanguinous marriage. On examination, he had trigonocephaly; anteverted nostrils, long philtrum and hypoplastic supraorbital ridges. X-ray showed sutural separation. Karyotyping confirmed deletion of short arm of chromosome 9 distal to band p22.

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Year:  1994        PMID: 8568717

Source DB:  PubMed          Journal:  J Postgrad Med        ISSN: 0022-3859            Impact factor:   1.476


  1 in total

1.  Child with deletion 9p syndrome presenting with craniofacial dysmorphism, developmental delay, and multiple congenital malformations.

Authors:  Nirmala D Sirisena; U Kalpani S Wijetunge; Ramya de Silva; Vajira H W Dissanayake
Journal:  Case Rep Genet       Date:  2013-07-25
  1 in total

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